Summary Structural details Experimental details Functional details Sequence Neighbor History Downloads

2IBW

Crystallographic and kinetic studies of human mitochondrial acetoacetyl-CoA thiolase (T2): the importance of potassium and chloride for its structure and function

Functional Information from GO Data

Chain	GOid	namespace	contents
A	0001889	biological_process	liver development
A	0003985	molecular_function	acetyl-CoA C-acetyltransferase activity
A	0005739	cellular_component	mitochondrion
A	0005759	cellular_component	mitochondrial matrix
A	0005783	cellular_component	endoplasmic reticulum
A	0006085	biological_process	acetyl-CoA biosynthetic process
A	0006550	biological_process	L-isoleucine catabolic process
A	0006629	biological_process	lipid metabolic process
A	0006631	biological_process	fatty acid metabolic process
A	0006635	biological_process	fatty acid beta-oxidation
A	0009725	biological_process	response to hormone
A	0015936	biological_process	coenzyme A metabolic process
A	0015937	biological_process	coenzyme A biosynthetic process
A	0016453	molecular_function	C-acetyltransferase activity
A	0016740	molecular_function	transferase activity
A	0016746	molecular_function	acyltransferase activity
A	0016747	molecular_function	acyltransferase activity, transferring groups other than amino-acyl groups
A	0019899	molecular_function	enzyme binding
A	0030955	molecular_function	potassium ion binding
A	0034736	molecular_function	cholesterol O-acyltransferase activity
A	0042594	biological_process	response to starvation
A	0042802	molecular_function	identical protein binding
A	0046356	biological_process	acetyl-CoA catabolic process
A	0046872	molecular_function	metal ion binding
A	0046952	biological_process	ketone body catabolic process
A	0060612	biological_process	adipose tissue development
A	0070062	cellular_component	extracellular exosome
A	0072229	biological_process	metanephric proximal convoluted tubule development
A	0120225	molecular_function	coenzyme A binding
A	1902224	biological_process	ketone body metabolic process
A	1902860	biological_process	propionyl-CoA biosynthetic process
B	0001889	biological_process	liver development
B	0003985	molecular_function	acetyl-CoA C-acetyltransferase activity
B	0005739	cellular_component	mitochondrion
B	0005759	cellular_component	mitochondrial matrix
B	0005783	cellular_component	endoplasmic reticulum
B	0006085	biological_process	acetyl-CoA biosynthetic process
B	0006550	biological_process	L-isoleucine catabolic process
B	0006629	biological_process	lipid metabolic process
B	0006631	biological_process	fatty acid metabolic process
B	0006635	biological_process	fatty acid beta-oxidation
B	0009725	biological_process	response to hormone
B	0015936	biological_process	coenzyme A metabolic process
B	0015937	biological_process	coenzyme A biosynthetic process
B	0016453	molecular_function	C-acetyltransferase activity
B	0016740	molecular_function	transferase activity
B	0016746	molecular_function	acyltransferase activity
B	0016747	molecular_function	acyltransferase activity, transferring groups other than amino-acyl groups
B	0019899	molecular_function	enzyme binding
B	0030955	molecular_function	potassium ion binding
B	0034736	molecular_function	cholesterol O-acyltransferase activity
B	0042594	biological_process	response to starvation
B	0042802	molecular_function	identical protein binding
B	0046356	biological_process	acetyl-CoA catabolic process
B	0046872	molecular_function	metal ion binding
B	0046952	biological_process	ketone body catabolic process
B	0060612	biological_process	adipose tissue development
B	0070062	cellular_component	extracellular exosome
B	0072229	biological_process	metanephric proximal convoluted tubule development
B	0120225	molecular_function	coenzyme A binding
B	1902224	biological_process	ketone body metabolic process
B	1902860	biological_process	propionyl-CoA biosynthetic process
C	0001889	biological_process	liver development
C	0003985	molecular_function	acetyl-CoA C-acetyltransferase activity
C	0005739	cellular_component	mitochondrion
C	0005759	cellular_component	mitochondrial matrix
C	0005783	cellular_component	endoplasmic reticulum
C	0006085	biological_process	acetyl-CoA biosynthetic process
C	0006550	biological_process	L-isoleucine catabolic process
C	0006629	biological_process	lipid metabolic process
C	0006631	biological_process	fatty acid metabolic process
C	0006635	biological_process	fatty acid beta-oxidation
C	0009725	biological_process	response to hormone
C	0015936	biological_process	coenzyme A metabolic process
C	0015937	biological_process	coenzyme A biosynthetic process
C	0016453	molecular_function	C-acetyltransferase activity
C	0016740	molecular_function	transferase activity
C	0016746	molecular_function	acyltransferase activity
C	0016747	molecular_function	acyltransferase activity, transferring groups other than amino-acyl groups
C	0019899	molecular_function	enzyme binding
C	0030955	molecular_function	potassium ion binding
C	0034736	molecular_function	cholesterol O-acyltransferase activity
C	0042594	biological_process	response to starvation
C	0042802	molecular_function	identical protein binding
C	0046356	biological_process	acetyl-CoA catabolic process
C	0046872	molecular_function	metal ion binding
C	0046952	biological_process	ketone body catabolic process
C	0060612	biological_process	adipose tissue development
C	0070062	cellular_component	extracellular exosome
C	0072229	biological_process	metanephric proximal convoluted tubule development
C	0120225	molecular_function	coenzyme A binding
C	1902224	biological_process	ketone body metabolic process
C	1902860	biological_process	propionyl-CoA biosynthetic process
D	0001889	biological_process	liver development
D	0003985	molecular_function	acetyl-CoA C-acetyltransferase activity
D	0005739	cellular_component	mitochondrion
D	0005759	cellular_component	mitochondrial matrix
D	0005783	cellular_component	endoplasmic reticulum
D	0006085	biological_process	acetyl-CoA biosynthetic process
D	0006550	biological_process	L-isoleucine catabolic process
D	0006629	biological_process	lipid metabolic process
D	0006631	biological_process	fatty acid metabolic process
D	0006635	biological_process	fatty acid beta-oxidation
D	0009725	biological_process	response to hormone
D	0015936	biological_process	coenzyme A metabolic process
D	0015937	biological_process	coenzyme A biosynthetic process
D	0016453	molecular_function	C-acetyltransferase activity
D	0016740	molecular_function	transferase activity
D	0016746	molecular_function	acyltransferase activity
D	0016747	molecular_function	acyltransferase activity, transferring groups other than amino-acyl groups
D	0019899	molecular_function	enzyme binding
D	0030955	molecular_function	potassium ion binding
D	0034736	molecular_function	cholesterol O-acyltransferase activity
D	0042594	biological_process	response to starvation
D	0042802	molecular_function	identical protein binding
D	0046356	biological_process	acetyl-CoA catabolic process
D	0046872	molecular_function	metal ion binding
D	0046952	biological_process	ketone body catabolic process
D	0060612	biological_process	adipose tissue development
D	0070062	cellular_component	extracellular exosome
D	0072229	biological_process	metanephric proximal convoluted tubule development
D	0120225	molecular_function	coenzyme A binding
D	1902224	biological_process	ketone body metabolic process
D	1902860	biological_process	propionyl-CoA biosynthetic process

Functional Information from PDB Data

site_id	AC1
Number of Residues	2
Details	BINDING SITE FOR RESIDUE CL B 2001

Chain	Residue
A	ASN414
B	CYS119

site_id	AC2
Number of Residues	3
Details	BINDING SITE FOR RESIDUE CL A 2002

Chain	Residue
A	CYS119
B	ASN414
B	HOH6025

site_id	AC3
Number of Residues	2
Details	BINDING SITE FOR RESIDUE CL D 2003

Chain	Residue
C	ASN414
D	CYS119

site_id	AC4
Number of Residues	4
Details	BINDING SITE FOR RESIDUE CL C 2004

Chain	Residue
D	HOH6028
D	HOH6087
C	CYS119
D	ASN414

site_id	AC5
Number of Residues	6
Details	BINDING SITE FOR RESIDUE K A 3001

Chain	Residue
A	TYR219
A	ALA280
A	ALA281
A	ALA283
A	VAL381
A	HOH6155

site_id	AC6
Number of Residues	6
Details	BINDING SITE FOR RESIDUE K B 3002

Chain	Residue
B	TYR219
B	ALA280
B	ALA281
B	ALA283
B	VAL381
B	HOH6076

site_id	AC7
Number of Residues	6
Details	BINDING SITE FOR RESIDUE K C 3003

Chain	Residue
C	TYR219
C	ALA280
C	ALA281
C	ALA283
C	VAL381
C	HOH6030

site_id	AC8
Number of Residues	6
Details	BINDING SITE FOR RESIDUE K D 3004

Chain	Residue
D	TYR219
D	ALA280
D	ALA281
D	ALA283
D	VAL381
D	HOH6082

site_id	AC9
Number of Residues	18
Details	BINDING SITE FOR RESIDUE COA A 6001

Chain	Residue
A	LEU184
A	HIS192
A	TYR219
A	ARG258
A	VAL259
A	ASP260
A	LYS263
A	LEU267
A	ALA281
A	SER284
A	ALA355
A	PHE356
A	MES5001
A	HOH6116
A	HOH6155
A	HOH6247
A	HOH6337
C	HOH6036

site_id	BC1
Number of Residues	17
Details	BINDING SITE FOR RESIDUE COA B 6002

Chain	Residue
B	LEU184
B	HIS192
B	TYR219
B	ARG258
B	VAL259
B	ASP260
B	LYS263
B	LEU267
B	ALA281
B	SER284
B	ALA355
B	PHE356
B	HOH6047
B	HOH6076
B	HOH6078
B	HOH6166
D	HOH6064

site_id	BC2
Number of Residues	16
Details	BINDING SITE FOR RESIDUE COA C 6003

Chain	Residue
A	HOH6237
C	LEU184
C	HIS192
C	TYR219
C	ARG258
C	VAL259
C	ASP260
C	LYS263
C	LEU267
C	PHE271
C	ALA280
C	SER284
C	ALA355
C	PHE356
C	HOH6030
C	HOH6081

site_id	BC3
Number of Residues	19
Details	BINDING SITE FOR RESIDUE COA D 6004

Chain	Residue
D	ALA355
D	PHE356
D	HIS385
D	HOH6052
D	HOH6065
D	HOH6082
B	HOH6154
D	LEU184
D	HIS192
D	TYR219
D	ARG258
D	VAL259
D	ASP260
D	LYS263
D	LEU267
D	PHE271
D	ALA280
D	ALA281
D	SER284

site_id	BC4
Number of Residues	8
Details	BINDING SITE FOR RESIDUE MES A 5001

Chain	Residue
A	PHE55
A	LEU56
A	LEU286
A	COA6001
A	HOH6046
A	HOH6346
C	TYR170
C	HOH6053

site_id	BC5
Number of Residues	9
Details	BINDING SITE FOR RESIDUE GOL A 4001

Chain	Residue
A	ALA201
A	LYS202
A	ASN205
A	ILE206
A	THR277
A	HOH6127
A	HOH6146
A	HOH6185
A	HOH6279

Functional Information from PROSITE/UniProt

site_id	PS00098
Number of Residues	19
Details	THIOLASE_1 Thiolases acyl-enzyme intermediate signature. INKvCASGMkAImmasqsL

Chain	Residue	Details
A	ILE122-LEU140

site_id	PS00099
Number of Residues	14
Details	THIOLASE_3 Thiolases active site. GLASICNGgGgAsA

Chain	Residue	Details
A	GLY408-ALA421

site_id	PS00737
Number of Residues	17
Details	THIOLASE_2 Thiolases signature 2. NinGGaVSlGHPiGmSG

Chain	Residue	Details
A	ASN375-GLY391

Functional Information from SwissProt/UniProt

site_id	SWS_FT_FI1
Number of Residues	4
Details	Active site: {"description":"Acyl-thioester intermediate","evidences":[{"source":"PubMed","id":"17371050","evidenceCode":"ECO:0000305"}]}

Chain

Residue

Details

site_id	SWS_FT_FI2
Number of Residues	4
Details	Active site: {"description":"Proton donor/acceptor","evidences":[{"source":"PubMed","id":"17371050","evidenceCode":"ECO:0000305"}]}

Chain

Residue

Details

site_id	SWS_FT_FI3
Number of Residues	36
Details	Binding site: {"evidences":[{"source":"PubMed","id":"17371050","evidenceCode":"ECO:0000269"}]}

Chain

Residue

Details

site_id	SWS_FT_FI4
Number of Residues	4
Details	Site: {"description":"Increases nucleophilicity of active site Cys","evidences":[{"source":"PubMed","id":"17371050","evidenceCode":"ECO:0000305"}]}

Chain

Residue

Details

site_id	SWS_FT_FI5
Number of Residues	32
Details	Modified residue: {"description":"N6-succinyllysine; alternate","evidences":[{"source":"UniProtKB","id":"Q8QZT1","evidenceCode":"ECO:0000250"}]}

Chain

Residue

Details

site_id	SWS_FT_FI6
Number of Residues	16
Details	Modified residue: {"description":"N6-succinyllysine","evidences":[{"source":"UniProtKB","id":"Q8QZT1","evidenceCode":"ECO:0000250"}]}

Chain

Residue

Details

site_id	SWS_FT_FI7
Number of Residues	4
Details	Modified residue: {"description":"N6-acetyllysine","evidences":[{"source":"PubMed","id":"19608861","evidenceCode":"ECO:0007744"}]}

Chain

Residue

Details

site_id	SWS_FT_FI8
Number of Residues	12
Details	Modified residue: {"description":"N6-acetyllysine","evidences":[{"source":"UniProtKB","id":"Q8QZT1","evidenceCode":"ECO:0000250"}]}

Chain

Residue

Details

Catalytic Information from CSA

site_id	CSA1
Number of Residues	3
Details	Annotated By Reference To The Literature 1afw

Chain	Residue	Details
A	GLY415
A	HIS385
A	CYS413

site_id	CSA2
Number of Residues	3
Details	Annotated By Reference To The Literature 1afw

Chain	Residue	Details
B	GLY415
B	HIS385
B	CYS413

site_id	CSA3
Number of Residues	3
Details	Annotated By Reference To The Literature 1afw

Chain	Residue	Details
C	GLY415
C	HIS385
C	CYS413

site_id	CSA4
Number of Residues	3
Details	Annotated By Reference To The Literature 1afw

Chain	Residue	Details
D	GLY415
D	HIS385
D	CYS413

site_id	CSA5
Number of Residues	2
Details	Annotated By Reference To The Literature 1afw

Chain	Residue	Details
A	HIS385
A	CYS413

site_id	CSA6
Number of Residues	2
Details	Annotated By Reference To The Literature 1afw

Chain	Residue	Details
B	HIS385
B	CYS413

site_id	CSA7
Number of Residues	2
Details	Annotated By Reference To The Literature 1afw

Chain	Residue	Details
C	HIS385
C	CYS413

site_id	CSA8
Number of Residues	2
Details	Annotated By Reference To The Literature 1afw

Chain	Residue	Details
D	HIS385
D	CYS413

		Sequence (fasta)
		PDBx/mmCIF
		PDBML format (no-atom)
		PDB format (full)
		Validation report (PDF)
		EDMap 2fo-fc (MTZ)